Canonical Allele Identifier: CA2077166009
Gene: GJB6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20231107G= , CM000675.2:g.20231107G= GRCh38
NC_000013.10:g.20805246G= , CM000675.1:g.20805246G= GRCh37
NC_000013.9:g.19703246G= NCBI36
NG_008323.1:g.6289C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241124.11:c.-427C= ENSP00000241124.6:n.-427C=
ENST00000400066.8:c.-186+275C= ENSP00000382939.3:n.-186+275C=
ENST00000643121.1:c.-381-46C= ENSP00000494468.1:n.-381-46C=
ENST00000643211.1:c.-302+275C= ENSP00000495841.1:n.-302+275C=
ENST00000644236.1:c.-258+275C= ENSP00000494122.1:n.-258+275C=
ENST00000644283.1:c.-186+275C= ENSP00000495320.1:n.-186+275C=
ENST00000647029.1:c.-296+275C= MANE Select ENSP00000493834.1:n.-296+275C=
ENST00000647243.1:c.-296+275C= ENSP00000494733.1:n.-296+275C=
ENST00000356192.6:c.-296+275C= ENSP00000348521.6:n.-296+275C=
ENST00000400065.7:c.-186+1087C= ENSP00000382938.3:n.-186+1087C=
ENST00000400066.7:c.-186+275C= ENSP00000382939.3:n.-186+275C=
NM_001110219.2:c.-296+275C= NP_001103689.1:n.-296+275C=
NM_001110220.2:c.-186+275C= NP_001103690.1:n.-186+275C=
NM_001110221.2:c.-186+1087C= NP_001103691.1:n.-186+1087C=
NM_006783.4:c.-427C= NP_006774.2:n.-427C=
NM_001110219.3:c.-296+275C= MANE Select NP_001103689.1:n.-296+275C=
NM_001370090.1:c.-302+275C= NP_001357019.1:n.-302+275C=
NM_001370091.1:c.-186+275C= NP_001357020.1:n.-186+275C=
NM_001370092.1:c.-296+275C= NP_001357021.1:n.-296+275C=
NM_001110220.3:c.-186+275C= NP_001103690.1:n.-186+275C=
NM_001110221.3:c.-186+1087C= NP_001103691.1:n.-186+1087C=